Column Setup Research Articles

Defluoridation of Groundwater Using Low-cost Adsorbents

Excessive fluoride in groundwater poses significant health risks to millions of people worldwide, necessitating effective and accessible defluoridation methods. This study investigates the use of column filtration for removing fluoride from groundwater. The study employs a systematic approach to evaluate the performance of different adsorbent materials in a fixed-bed column setup. Various materials were tested as adsorbents in column, including Brick powder, Neem leaf powder, Lime, Sawdust, and Vetiver. The research examines the effects of key operational parameters such as bed depth, flow rate, and initial fluoride concentration on the overall removal efficiency. Experiments were conducted using groundwater to assess the method's effectiveness. Results indicated that column filtration can effectively reduce fluoride concentrations to below the World Health Organization's recommended limit of 1.5 mg/L. This report contributes to the development of efficient, cost-effective, and sustainable solutions for groundwater defluoridation. All adsorbents used were inexpensive materials, available easily in nature and locally at village or rural level. Some of the adsorbents were very effective in removal of fluoride ion and can be used as defluoridating agents but they impart color and turbidity to the groundwater. Among all the adsorbents used, Vetiver demonstrated higher removal efficiency of 78% followed up by limestone 77% removal but hindered by its precipitation. Sawdust and brick powder were also efficient up to a certain extent of 72% and 69% respectively in adsorbing fluoride ions. Neem leaves powder was found to be least effective in adsorbing showing about 50% removal efficiency.

Conceptual and Applied Aspects of Water Retention Tests on Tailings Using Columns

The water retention capacity of porous materials is crucial in various geotechnical and environmental engineering applications such as slope stability analysis, landfill management, and mining operations. Filtered tailings stacks are considered an alternative to traditional tailings dams. Nevertheless, the mechanical behaviour and stability of the material under different water content conditions are of concern because these stacks can reach considerable heights. The water behaviour in these structures is poorly understood, particularly the effects of the water content on the stability and potential for liquefaction of the stacks. This study aims to investigate the water retention and flow characteristics of compacted iron ore tailings in high columns to better understand their hydromechanical behaviour. The research used 5 m high columns filled with iron ore tailings from the Quadrilátero Ferrífero region in Minas Gerais, Brazil. The columns were prepared in layers, compacted, and instrumented with moisture content sensors and suction sensors to monitor the water movement during various stages of saturation, drainage, infiltration, and evaporation. The sensors provided consistent data and revealed that the tailings exhibited high drainage capacity. The moisture content and suction profiles were effectively established over time and revealed the dynamic water retention behaviour. The comparison of the data with the theoretical soil water retention curve (SWRC) demonstrated a good correlation which indicates that there was no hysteresis in the material response. The study concludes that the column setup effectively captures the water retention and flow characteristics of compacted tailings and provides valuable insights for the hydromechanical analysis of filtered tailings stacks. These findings can significantly help improve numerical models, calibrate material parameters, and contribute to the safer and more efficient management of tailings storage facilities.

Spent coffee waste-derived biochar improves physical properties, water retention, and maize (Zea mays L.) growth in sandy soil

Adding organic soil amendments can improve the physical and hydrological properties of soil, subsequently enhancing fertility for better crop production. In this study, spent Arabica and Columbian coffee wastes and their respective biochars were evaluated as soil amendments to improve the physical and hydrological properties of loamy sand soil and enhance maize (Zea mays L.) crop growth. Spent Arabica coffee (AC) and Columbian coffee (CC) wastes were collected and transformed into biochar through pyrolysis process at 550 °C with a residence time of 3 h and pyrolysis rate of 5 °C per minute. The AC and CC derived biochar were termed as ABC and CBC, respectively. The produced soil amendments were applied to soil at 0% (control), 1%, 3%, and 5% in a column setup. The moisture characteristics, including water infiltration, evaporation, and water retention, were investigated. Thereafter, the prepared amendments were applied to loamy sand soils at 0% (control), 1%, 3%, and 5% (w/w) application rates. Maize growth was then observed for a period of 30 days under greenhouse conditions. Results of the column trials showed that ABC and CBC applied at 5% reduced the cumulative water evaporation by 57%–66% and cumulative infiltration by 124%–181% compared to control. Likewise, 5% application of ABC and CBC resulted in 101 to 130% higher water retention in loamy sand soil. Results of the greenhouse experiment showed that 5% application of ABC and CBC amendments resulted in root biomass of 2.12 and 2.38 g, respectively, as compared to 0.51 g in control treatment. Similar treatments resulted in shoot biomass of 9.70 and 9.93 g respectively, as compared to 7.37 g in control. Likewise, 5% application of CBC and ABC increase plant height from 15.71 to 30.94 cm in ABC and 33.23 cm in CBC. Overall, 5% application of coffee waste-derived biochars significantly reduced water evaporation and infiltration, while increasing soil water retention and maize plant height, root biomass, and shoot biomass. Therefore, spent coffee waste-derived biochar could effectively be employed to improve physical and hydrological properties of loamy sand soils for better crop productivity.

Extracting metal ions from basic oxygen steelmaking dust by using bio-hydrometallurgy

This study aimed to optimise metal extraction from secondary hazardous sources, such as basic oxygen steelmaking dust (BOS-D). Initially, three batch systems approaches, including bioleaching using Acidithiobacillus ferrooxidans, chemical leaching using choline chloride-ethylene glycol (ChCl-EG) and a combined approach were compared. Then, scaling up was evaluated through a semi-continuous bioleaching column system with varied leachate recirculation over 21 days, focusing on Y, Ce, Nd, Li, Co, Cu, Zn, Mn, and Al. Bioleaching outperformed the control experiments within 3 days in the batch, demonstrating the key role of A. ferrooxidans. Chemical leaching conducted with a solid concentration of 12.5 % (w/v) successfully dissolved over 50 % of all metals within 2 h. For rare earth elements (REE), both bioleaching and hybrid leaching outperformed chemical leaching. However, considering factors such as process duration, overall efficiency, and ease of extraction, chemical leaching was the most effective method. Leachate recirculation reached a plateau after 11 days, resulting in extraction efficiency of 39 % when semi-continuous column set-up was used. Interestingly, variations in recirculation rates did not influence the extraction efficiency. Overall, this study emphasizes the considerable potential of bioleaching for metal recovery, but also highlights the need for further studies for enhancing permeability for percolation methods and optimisation, particularly in parameters such as aeration rate, when transitioning to larger scale systems.

Towards a mechanistic model of oxidase deactivation in a bubble column

Despite the many advantages of biocatalysis, enzyme stability remains an issue. This work investigates the long-term kinetic stability of a water-forming NAD(P)H-oxidase (NOX2), an enzyme of potential industrial interest for NAD(P)H regeneration, in a bubble column sparged with air, which enables reasonable oxygen transfer but without drastic enzyme deactivation. Experiments have been performed with the particular goal of explaining the observed two-stage deactivation trend. We show evidence supporting the hypothesis that the first stage is related to the adsorption of enzymes to the interface, followed by a subsequent deactivation stage at the interface.The characterization of NOX deactivation in the bubble column setup, complemented by additional’quiescent’ experiments, has enabled the development of a first principles model as the first step towards a complete mechanistic model of oxidase deactivation at gas–liquid interfaces.

Arsenate removal using chitosan-coated bentonite via fixed-bed system: a process integration by fuzzy optimization.

Groundwater contamination is a global concern that has detrimental effect on public health and the environment. Sustainable groundwater treatment technologies such as adsorption require attaining a high removal efficiency at a minimal cost. This study investigated the adsorption of arsenate from groundwater utilizing chitosan-coated bentonite (CCB) under a fixed-bed column setup. Fuzzy multi-objective optimization was applied to identify the most favorable conditions for process variables, including volumetric flow rate, initial arsenate concentration, and CCB dosage. Empirical models were employed to examine how initial concentration, flow rate, and adsorbent dosage affect adsorption capacity at breakthrough, energy consumption, and total operational cost during optimization. The ε-constraint process was used in identifying the Pareto frontier, effectively illustrating the trade-off between adsorption capacity at breakthrough and the cost of the fixed-bed system. The integration of fuzzy optimization for adsorption capacity and its total operating cost utilized the global solver function in LINGO 20 software. A crucial equation derived from the Box-Behnken design and a cost equation based on energy and material usage in the fixed-bed system was employed. The results from identifying the Pareto front determined boundary limits for adsorption capacity at breakthrough (ranging from 12.96 ± 0.19 to 12.34 ± 0.42μg/g) and total operating cost (ranging from 955.83 to 1106.32 USD/kg). An overall satisfaction level of 35.46% was achieved in the fuzzy optimization process. This results in a compromise solution of 12.90μg/g for adsorption capacity at breakthrough and 1052.96 USD/kg for total operating cost. Henceforth, this can allow a suitable strategic decision-making approach for key stakeholders in future applications of the adsorption fixed-bed system.

Adsorption of Radioactive Iodine Using Nanocarbon on ETS-10 as Adsorbent

Laboratory-synthesized nanocarbon pelletized with titanosilicate (ETS-10) as a support matrix has been investigated for the capture of radioactive iodine present as methyl iodide (CH3I) in the off-gas streams produced during aqueous reprocessing of used nuclear fuel. The mass fraction of carbon in the sorbent matrix was 0.10. The effects of residence time and CH3I concentration were investigated using a continuous flow column setup to quantify the adsorption and desorption capacities of adsorbent under dynamic conditions from an air stream containing CH3I present at concentrations representative of those expected in the off-gas streams. Air with CH3I gas as a source in the column resulted in quantifiable CH3I adsorption with 0.98 mg/g of adsorption capacity. Laboratory-made nanocarbons had a larger adsorption capacity than those of the other carbons reported in the literature. Additionally, the adsorption capacity of nanocarbon on ETS-10 is compared to that of nanocarbon coated on cordierite in previous studies.

Optimization of elution conditions and comparison of emerging biocompatible columns on the resolving power and detection sensitivity of oligonucleotides by ion-pairing reversed-phase liquid chromatography mass spectrometry

A generic performance comparison strategy has been developed to evaluate the impact of mobile-phase additives (ion-pairing agent / counter ion systems), distinct stationary phases on resulting resolving power, and MS detectability of oligonucleotides and their critical impurities in gradient IP-RPLC. Stationary-phase considerations included particle type (core-shell vs. fully porous particles), particle diameter, and pore size. Separations were carried out at 60°C to optimize mass transfer (C-term). The incorporation of an active column preheater mitigated thermal mismatches, leading to narrower peaks and overcoming peak splitting. Acetonitrile as organic modifier outweighed methanol in terms of peak-capacity generation and yielded a 30% lower back pressure. Performance screening experiments were conducted varying ion-pairing agents and counter ions, while adjusting gradient span achieved an equivalent effective retention window. Hexafluoromethylisopropanol yielded superior chromatographic resolution, whereas hexafluoroisopropanol yielded significantly higher MS detection sensitivity. The 1.7 µm core-shell particle columns with 100 Å pores provided maximum resolving power for small (15–35 mers) oligonucleotides. Sub-min analysis for 15–35 polyT ladders was achieved operating a 50 mm long column at the kinetic performance limits. High-resolution separations between a 21-mer modified RNA sequence oligonucleotides and its related (shortmer and phosphodiester) impurities and complementary strand were obtained using a coupled column set-up with a total length of 450 mm.

Conversion of char from pyrolysis of plastic wastes into alternative activated carbons for heavy metal removal

The valorization of post-consumer mixed plastics in pyrolysis processes represents an abundant reservoir of carbon that can be effectively converted into useful chars. This process not only holds appeal in terms of improving plastic waste concerns but also contributes to the reduction of greenhouse gas emissions, thus aligning with the principles of a circular economy paradigm. In this study, the char produced from the pyrolysis of post-consumer mixed plastic waste has been activated with Na2CO3, KOH, NaOH, and K2CO3 to improve the textural, structural, and composition characteristics, leading to improved adsorption capability. These characteristics were studied by N2 adsorption-desorption isotherms, scanning electron microscopy, elemental and immediate analysis, and X-ray photoelectron spectroscopy. The developed surface area (SBET) was 573, 939, 704 and 592 m2 g−1 for Na2CO3, KOH, NaOH and K2CO3 activated carbons, respectively. These activated chars (ACs) were tested for the adsorption of heavy metals in both synthetic waters containing Pb, Cd, and Cu and industrial wastewater collected at an agrochemical production plant. Na2CO3-AC was the best performing material. The metal uptake in synthetic waters using a batch set-up was 40, 13 and 12 mg g−1 for Pb, Cd and Cu. Experiments in a column set-up using Na2CO3-AC resulted in a saturation time of 290, 16, and 80 min for Pb, Cd, and Cu synthetic waters, respectively, and metal uptakes of 26.8, 4.1, and 7.9 mg g−1, respectively.The agrochemical effluents, containing mainly Cr, Cu, Mn, and Zn were tested in a plug-flow column. The metal uptake notably decreased compared to synthetic water due to a competition effect for active sites.

3D electrical resistivity survey for reduction of groundwater drilling uncertainties in a clay-rich environment

Drilling for groundwater is expensive and challenging. It is even more challenging to find a location that will result in a high-yield well in heterogeneous environments. To tackle the heterogeneity issue, geophysical surveys can help in mapping the subsurface structure and delineating the drilling trajectory. The current study displays the effectiveness of 3D electrical resistivity tomography (ERT) to locate a permeable groundwater zone within a highly heterogeneous and clayey subsurface. Ground truthing the acquired geophysical data with in-situ sampling helps ensure accuracy in classifying groundwater zones in the final inverted 3D data set while also delineating boundaries between permeable groundwater zones and less permeable clayey structures. In-situ samples of groundwater and soil were used to measure the saturated region's resistivity in the laboratory using a column setup. Clay zones in the data set are classified from the nearby well data at similar depth ranges and from very low resistivity values from ERT data and laboratory measurements. The results display highly differentiating resistivity zones that are attributed to the scattered clay lenses (low resistivity) in conjunction with the freshwater zone (high resistivity). The distinction between clayey and nonclayey bodies is important to better inform drilling locations for optimal groundwater yield. This study concludes that with the aid of low-cost geophysical surveys and minimal in-situ sampling data correlations, permeable groundwater boundaries and clay lens volumes can be identified easily.

A Fixed Bed Adsorption Column Study for Synthetic Dye Wastewater using Magnetic Biochar

The study aimed to investigate the performance of a fixed bed column using magnetic biochar as an adsorbent for synthetic dye wastewater treatment. The magnetic biochar was synthesized by pyrolyzing paper mill sludge at 350 ℃ and modified with iron oxide nanoparticles to enhance its magnetic properties. The adsorption capacity of the magnetic biochar was evaluated using methylene blue (MB) dye in wastewater. In present study the fixed bed column adsorption was conducted using MBC to treat MB wastewater. A fixed bed column setup was utilized in the experiments, maintaining a continuous flow rate of 15 mL/min at various bed height (i.e. 2.5, 5 & 7cm). Breakthrough & exhaustion capacity for each three different bed height at constant flow rate was also carried out. The Yoon-Nelson and Thomas kinetics models were also used in order to understand the dynamic performance of the fixed bed column. the respectively. The results shows that Yoon-Nelson model fitted best for the experimental data approximately R2 value of 0.96 against Thomas model R2 value of 0.95. Hence, it can be concluded that fixed bed column with MBC performed best with higher bed height & adsorption process is limited by film & pore diffusion

Uranium biomineralization by immobilized Chryseobacterium sp. strain PMSZPI cells for efficient uranium removal

Uranium (U) contamination is hazardous to human health and the environment owing to its radiotoxicity and chemical toxicity and needs immediate attention. In this study, the immobilized biomass of Chryseobacterium sp. strain PMSZPI isolated from U enriched site, was investigated for U(VI) biomineralization in batch and column set-up. Under batch mode, the fresh or lyophilized cells successfully entrapped in calcium alginate beads demonstrated effectual U precipitation under acid and alkaline conditions. The maximum removal was detected at pH 7 wherein ∼98–99% of uranium was precipitated from 1 mM uranyl carbonate solution loading ∼350 mg U/g of biomass within 24 h in the presence of organic phosphate substrate. The resulting uranyl phosphate precipitates within immobilized biomass loaded beads were observed by SEM-EDX and TEM while the formation of U biomineral was confirmed by FTIR and XRD. Retention of phosphatase activity without any loss of uranium precipitation ability was observed for alginate beads with lyophilized biomass stored for 90 d at 4 °C. Continuous flow through experiment with PMSZPI biomass immobilized in polyacrylamide gel exhibited U loading of 0.8 g U/g of biomass at pH 7 using 1 l of 1 mM uranyl solution. This investigation established the feasibility for the application of immobilized PMSZPI biomass for field studies. Environmental implicationUranium contamination is currently a serious environmental concern owing to anthropogenic activities and needs immediate attention. We have developed here a biotechnological method for successful uranium removal using immobilized cells of a uranium tolerant environmental bacterium, Chryseobacterium sp. strain PMSZPI isolated from U ore deposit via phosphatase enzyme mediated uranium precipitation. The ability of immobilized PMSZPI cells to precipitate U(VI) as long-term stable U phosphates under environmental conditions relevant for contaminated waters containing high concentrations of U that exerts toxicity for biological systems is explored here. The long term stability of the immobilized biomass without compromising its U removal capacity shows the relevance of the bioremediation strategy for uranium contamination proposed in this work.

Removal of fluoride from groundwater by chemically functionalized sugarcane bagasse biochar and bagasse pellets in a fixed-bed sorption system

This study aimed to investigate the design parameters for a filter intended to remove fluoride from groundwater. Water fluoridation notably influences groundwater, particularly in arid and semi-arid areas that exacerbate the challenge of availability of safe drinking water from Groundwater resources in numerous developing nations. Experiments were conducted to determine the fluoride concentrations in groundwater sources in the arid region of Maharashtra, India. Samples were collected from seven villages in three districts of Maharashtra. This study utilized chemically functionalized sugarcane bagasse biochar adsorbent (SCBB), which is low-cost and easily accessible, to remove fluoride from groundwater in a column setup. The recommended design parameters for the packed-bed column flow rate (Q) are 100 ml min−1 and bed height (d) is 30 cm.

Non-derivatizing solvent assisted waste-derived cellulose/ MOF composite porous matrix for efficient metal ion removal: comprehensive analysis of batch and continuous packed-bed column sorption studies.

The use of metal-organic frameworks (MOFs) for wastewater treatment in continuous operation is a major challenge. To address this, the present study demonstrates the eco-friendly and economic synthesis of Ca-MOF immobilized cellulose beads (Ca-MOF-CB) derived from paper waste. The synthesized Ca-MOF-CB were characterized using standard analytical techniques. Batch sorption studies were performed to check the effect of cellulose composition (wt%), Ca-MOF loading, contact time, and initial metal ion (Pb2+, Cd2+, and Cu2+) concentration. Ca-MOF-CB beads exhibited outstanding equilibrium sorption capacities for Pb2+, Cd2+, and Cu2+, with estimated values of 281.22 ± 7.8, 104.01 ± 10.58, and 114.21 ± 9.68 mg g-1, respectively. Different non-linear isotherms and kinetic models were applied which confirmed the spontaneous, endothermic reactions for the physisorption of Pb2+, Cd2+, and Cu2+. Based on the highest equilibrium sorption capacity for Pb2+ ion, in-depth parametric column studies were conducted in an indigenously developed packed-bed column set-up. The effect of packed-bed height (10 and 20 cm), inlet flow rate (5 and 10 mL min-1), and inlet Pb2+ ion concentration (200, 300, and 500 mg L-1) were studied. The breakthrough curves obtained at different operating conditions were fitted with the empirical models viz. the bed depth service time (BDST), Yoon-Nelson, Thomas, and Yan to estimate the column design parameters. In order to determine the financial implications at large-scale industrial operations, an affordable synthesis cost of 1 kg of Ca-MOF-CB was estimated. Conclusively, the present study showed the feasibility of the developed Ca-MOF-CB for the continuous removal of metal ions at an industrial scale.

Enhancing wave energy harvesting: Performance analysis of a dual chamber oscillating water column

This study investigates the hydrodynamic characteristics of a dual chamber oscillating water column (OWC) setup through a series of experiments, aiming to assess its potential for harvesting wave energy. The investigation involves varying frontwall drafts, power take-off (PTO) dampings, and incident wave conditions, while quantitatively evaluating the OWC system's performance using the capture width ratio (CWR) as the key metric. The findings indicate that the dual chamber configuration consistently exhibits enhanced performance for all combinations of orifice ratios, opening heights, and incident wave frequencies studied. As expected, increasing the opening height of the second chamber leads to improved performance of the OWC. Interestingly, the effect of varying applied PTO damping on improvement of CWR values is found to be relatively insensitive. The most significant improvements in CWR are observed for larger incident wave frequency values. For instance, for dimensionless wave frequency (Kh) values of 1.43 and 1.68, the CWR increases from 0.47 and 0.26 to 0.72 and 0.52, respectively, with the orifice ratio combination of τ1, 0.015, and τ2, 0.018. It is worth noting that the single chamber OWC operates most efficiently within the resonant frequency range of 0.94–1.23, while the dual chamber design extends this frequency range, enabling efficient wave energy capture over a wider spectrum of wave conditions. The dual chamber configuration offers considerable advantages for wave energy conversion applications by increasing the effective frequency bandwidth for optimal energy capture. The research findings suggest that this innovative design has the potential to significantly enhance the efficiency and adaptability of wave energy converters, contributing to the advancement of sustainable and renewable energy technologies.

Development of a molecularly imprinted membrane for selective, high-sensitive, and on-site detection of antibiotics in waters and drugs: Application for sulfamethoxazole

Sulfonamides are among the widespread bacterial antibiotics. Despite this, their quick emergence constitutes a serious problem for ecosystems and human health. Therefore, there is an increased interest in developing relevant detection method for antibiotics in different matrices. In this work, a straightforward, green, and cost-effective protocol was proposed for the preparation of a selective molecularly imprinted membrane (MIM) of sulfamethoxazole (SMX), a commonly used antibiotic. Thus, cellulose acetate was used as the functional polymer, while polyethylene glycol served as a pore-former. The developed MIM was successfully characterized through scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). The MIM was used as a sensing platform in conjunction with a smartphone for optical readout, enabling on-site, selective, and highly sensitive detection of SMX. In this way, a satisfactory imprinting factor of around 3.6 and a limit of detection of 2 ng mL−1 were reached after applying response surface methodologies, including Box-Behnken and central composite designs. Besides, MIM demonstrated its applicability for the accurate and selective detection of SMX in river waters, wastewater, and drugs. Additionally, the MIM was shown to be a valuable sorbent in a solid-phase extraction protocol, employing a spin column setup that offered rapid and reproducible results. Furthermore, the developed sensing platform exhibited notable regeneration properties over multiple cycles and long shelf-life in different storage conditions. The newly developed methodology is of crucial importance to overcome the limitations of classical imprinting polymers. Furthermore, the smartphone-based platform was used to surpass the typically expensive and complicated methods of detection.

Long-term phosphorus removal by Ca and Fe-rich drainage filter materials under variable flow and inlet concentrations

Phosphorus (P) losses from tile-drained agricultural fields may degrade surface water quality by accelerating eutrophication. Among the different edge-of-field technologies, compact filter systems using different filter materials have been identified as potentially effective solutions for removing P from drainage water before discharge downstream.This study investigated the long-term (>696 days) P removal efficiency of 5 different filter materials in a column setup, using artificial drainage water (pH 6). Filter materials included two iron-based granulates (calcinated diatomaceous earth (CDE), ferric hydroxide granules (CFH)), and three calcium-based granulates (seashells, limestone, calcinated silicate/calcium oxide (Filtralite-P)). Experiments were performed under variable flow rates (0.037 and 1.52 L h−1; hydraulic retention time of 26–43 min and 18–30 h) and inlet P concentrations (0.14 and 0.7 mg L−1). An overall analysis revealed that the Fe-based materials achieved higher P retention than Ca-based materials. In particular, CFH was capable of retaining 99 and 98 % of the high and low inlet P concentrations, respectively. Conversely, limestone retained only 25 % of the high P load. CDE performed moderately well, independently of the inlet P concentration. Filtralite-P and Seashells performed well at high inlet P concentration but relatively poorly at low P concentration. The sensitivity of filter material P removal efficiency to variations in P loading was generally lowest for CFH and highest for limestone.

Detection of Iron Disulfide Materials in Geological Porous Media Using Spectral Induced Polarization Method

Summary Iron sulfide (FeS) scale is a known problem that can significantly impact oil and gas (O&G) production. However, current monitoring methods cannot detect the problem at early stages, not until it is too late for any meaningful remedial action. Spectral induced polarization (SIP) is an established geophysical method increasingly used in near-surface environmental applications. The unique characteristics of the SIP method, mainly the sensitivity to both bulk and interfacial properties of the medium, allow for the potential use as a characterization and monitoring tool. SIP is particularly sensitive to metallic targets, such as FeS, with direct implications for the detection, characterization, and quantification of FeS scale. In a column setup, various concentrations of pyrite (FeS2), a common form of FeS scale, within calcite were tested to examine the SIP sensitivity and establish qualitative and quantitative relationships between SIP signals and FeS2 properties. The concentration of FeS2 in the samples directly impacts the SIP signals; the higher the concentration, the higher the magnitude of SIP parameters. Specifically, the SIP method detected the FeS2 presence as low as 0.25% in the bulk volume of the tested sample. This study supports the potential use of SIP as a detection method of FeS2 presence. Furthermore, it paves the way for upcoming studies utilizing SIP as a reliable and robust FeS scale characterization and monitoring method.

Small biochar particles hardly disintegrate under cryo-stress

Physical disintegration of biochar has been postulated to determine the persistence and mobility in soil of this recalcitrant carbon pool. Therein, freeze–thaw cycling can induce substantial physical stress to biochars. We here investigated the physical disintegration and subsequent mobilisation of five different biochars under “realistic worst-case scenarios” in a laboratory soil column setup as well as in shaking and sonication batch experiments. The mobilization of carbon from biochar particles (0.25–1 mm) was investigated in the absence of clay at a pH of 6.3 with and without 80 freeze–thaw cycles. The small biochar particles used in this study did not strongly disintegrate after freeze–thaw cycling, possibly because of freezing point depression in biochar micropores. Our results in comparison with findings in literature suggest that freeze–thaw-induced physical disintegration of biochar is a process more pronounced for large biochar particles containing substantial meso- and macropores. Biochars with larger ash fractions disintegrated more, presumably because of the ash-associated formation of unstable cavities within the biochar. Physical stability of biochars produced from the same feedstock at different pyrolysis temperatures decreased with increasing aromaticity, which may be linked to a higher rigidity of more aromatic structures. Moisture content in the soil increased carbon mobilization from biochar more than physical stress such as freeze–thaw cycling. The physical disintegration of biochar and subsequent mobilization of micro-and nanosized carbon should thus be considered of minor relevance and is often not a driving factor for biochar stability in soil.

USING N-OVEL COATED SAND AS REACTIVE BED IN PERMEABLE BARRIER FOR ELIMINATION OF METHYL ORANGE DYE FROM GROUNDWATER*

This study investigates the efficacy of sand coated with calcium / aluminum (Ca/Al)-layered double hydroxide (LDH) in the elimination of methyl orange dye from simulated groundwater using method of permeable reactive barrier. For green (sustainable) manufacturing of this sand, aluminum prepared from dissolution of alum (cheap coagulant) can be interacted chemically with calcium extracted from cement kiln dust byproduct to create nanoparticles of Ca and Al that precipitate on the filter sand. Sorption measurements for interaction of methyl orange dye and coated sand was well formulated by Langmuir model with highest value of correlation (determination coefficient= 0.999) and lowest errors (sum of squared errors= 0.0122). Also, the maximum capacity of adsorption was valued of 0.9453 mg/g and the sorption curve can classify as “favorable” type. According to desorption measurements, little percentage of dye (0.91%) can desorb from exhausted coated sand through washing with water due to strength of bonding between sorbent and dye molecules. Also, the exhausted sorbent can regenerate with efficiency not less than 85% after eight of regeneration cycles. Finally, measurements of breakthrough curves in the continuous mode operation using column setup proved that the propagation of dye front (and consequently the longevity of barrier) would increase significantly with thicker barrier and lowest values of influent concentration and flow rate. COMSOL (computer solution) package can use effectively in the simulation of these curves.